Strippable wax coating compositions

ABSTRACT

THIS INVENTION RELATES TO S STRIPPABLE WAX COATING CONTAINING AN ETHYLENE-VINYL ACETATE POLYMERIC COMPOSITION AND A STRIPPING AGENT WHICH IS EITHER AN N-SUBSTITUTED FATTY ACID AMIDE OR A NITROGEN CONTAINING COMPOUND CONTAINING A FATTY ACID RESIDUE. PARTICULARLY PREFERRED ARE WAX COMPOSITIONS WHICH CONTAIN AS THE STRIPPING AGENT AN N-SUBSTITUTED FATTY ACID AMIDE CONTAINING A FATTY ACID RESIDUE HAVING FROM 10 TO 17 CARBON ATOMS. THE COMPOSITIONS CAN ALSO CONTAIN MINOR AMOUNTS OF A MINERAL OIL TO INCREASE THE STRIPPABILITY.

United States Patent 3,714,094 STRJIPPABLE WAX COATING COMPOSITIONS Dominic Apikos, Park Forest, 1111., assignor to Atlantic Richfield Company, Philadelphia, Pa.

No Drawing. Application Jan. 12, 1970, Ser. No. 2,383, which is a division of appiication Ser. No. 556,555, June 10, 1966. Divided and this application Dec. 13, 1971, Ser. No. 207,699

Int. Cl. C08f 45/52 US. Cl. 260-28.5 AV

ABSCT OF THE DISCLOSURE 13 Claims CROSS REFERENCE TO RELATED APPLICATION This is a division, of application Ser. No. 2,383, filed Jan. 12, 1970; Ser. No. 2,383 is a division of my pending application, Ser. No. 556,555 filed June 10, 1966 now 3,518,215, entitled Strippable Wax Coating Compositions.

BACKGROUND OF INVENTION Strippable coatings are well-known in the art. They are utilized in applications wherein it is desirable to provide temporary surface protection against abrasion, rust, dirt and other damage occurring in storage and handling. After the necessary protection period has expired, it is desirable that these coatings be removed with a minimum of time and effort. These requirements have led to the development of various compositions which may be deposited as coatings upon a surface and thereafter removed as essentially continuous films. For example, polyvinyl chloride plastisols can be deposited, cured, and then peeled from a surface. This coating is very expensive and therefore, can only be economically deposited in thicknesses of a few mils. Furthermore, a strippable coating is produced only after the liquid plastisol has been properly cured at temperatures in the order of 300 F.

In order to eliminate the necessity of a cure, hot melt coatings have been produced from cellulosic materials such as ethyl cellulose in combination with large proportions of mineral oil. These compositions usually are quite odorous, have oily surface appearances and require coating temperatures in excess of 300 F. Other hot melt coatings such as those made from wax alone are not strippable. The addition of various polymers including ethylene-vinyl acetate copolymers imparts physical strength to the wax film but it also increases the adhesive bond between the surface and the film. In order to impart strippability, various additives such as mineral oil, fluorinated compounds, silicones and partial esters have been incorporated into these wax-polymer compositions. These additives either impart high cost, poor coating appearance or necessitate extensive coating techniques.

It has now been found that outstanding strippable coatings can be produced by combining wax with ethylene vinyl acetate copolymers and minor amounts of certain nitrogen-containing compounds. These compositions offer excellent strippability, low cost and they do 3,714,04 Patented Jan. 30, 19?.3

not require complex coating processes. The coating compositions of this invention can be economically applied in considerable thicknesses using a hot melt technique without need of any subsequent cure.

The compositions of this invention may be used to protect the surfaces of metals such as aluminum, steel, Zinc, brass, and chromium or the surfaces of various plastic or synthetic products such as laminates of phenolforinaldehyde, melamine-formaldehyde and urea-formaldehyde resins, phonograph records, and the surfaces of many natural products such as wood paneling, flooring strips and the like. In general, the compositions of this invention may be utilized on any solid surface, such as glass, ceramic or mica, which forms a minimum adhesive bond with the coating.

It is an object of this invention to provide wax compositions which may be deposited upon a surface and the eafter completely removed from the surface as essentially continuous films.

It is a further object of this invention to provide articles of manufacture which have these strippable wax compositions deposited upon their surfaces.

The compositions of this invention comprise in parts by weight:

(A) parts of wax; and,

(B) from 10 to 300 parts of a polymeric composition consisting essentially of:

(i) from 40-100 weight percent of an ethylenevinyl acetate copolymer wherein the vinyl acetate content ranges from 15-35 weight percent, and

(ii) from 0-60 weight percent of a compound which is a plasticizer for this ethylene-vinyl acetate copolymer,

(C) In an amount sufficient to impart strippability at least one stripping agent selected from the group consisting of (i) an N-substituted fatty acid amide having a structural formula:

0 Ri'iN(CH2)nC 0 OM wherein R is an aliphatic radical containing 10 30 carbon atoms, R is an alkyl group containing 1-4 carbon atoms, n is an integer from 1-4 and M is selected from the group consisting of hydrogen and alkali metals having an atomic number of less than 20.

(ii) a nitrogen containing compound having the following structural formula:

wherein W is a radical selected from the group consisting ofhydrogen and an alkyl radical containing 1-6 carbon atoms, R" is hydrogen or a methyl radical, Z is a radical selected from the group consisting of o R%, and RN(CH2) wherein R is an aliphatic radical containing 10- 30 carbon atoms and t is an integer from l6, and R" is hydrogen or a methyl radical. (D) from 020 parts of a hydrocarbon oil having a viscosity at 210 F. in excess of 25 SSU.

The N-substituted fatty acid amides and the nitrogen containing compounds must be present in the composition within a certain critical concentration range. The concentration must be sufficient to impart strippability without completely destroying the bond between the surface and the coating. In order to be considered strippable, it is necessary that the coating be capable of being totally removed from the surface as essentially continuous films. These critical concentrations are dependent upon the type of stripping agent utilized, the type and amount of other components present, and the degrees of strippability desired. In most compositions, strippability is obtained with concentrations as low as 0.5 part by weight in 100 parts wax. Concentrations which range from 1-5 parts by weight per 100 parts wax have been found to be most satisfactory. Higher concentrations, while operable, are accompanied by substantial migration to the surface of the coating. The extent of this migration varies with the particular strippng agent and in general is related to its wax compatibility. This migration may totally destroy the adhesive bond, or provide an unattractive coating appearance and feel.

The N-substituted fatty acid amides which can be utilized in the practice of this invention have the following structural formula:

wherein M is hydrogen or an alkali metal having an atomic number of less than 20. Preferably M is hydrogen or sodium and most preferably, it is hydrogen. n is an integer from 1-4 and preferably is 1, R is an alkyl group containing 1-4 carbon atoms preferably, methyl. R is an aliphatic radical containing to 30 carbon atoms, and can be saturated or unsaturated, and linear or branched chain. It can be derived from the hydrocarbon residues of monocarboxylic fatty acids. These hydrocarbon residues can be substituted with a pendant oxygen atom such as a keto or hydroxyl group or an ester linkage. Suitable hydrocarbon residues which can be utilized include but are not limited to the residues derived from saturated acids such as n-undecyclic, lauric,. myristic, n-pentadecyclic, palmitic, margaric, stearic, avachidic, 'behenic, lignoceric, cerotic, n-heptacosoic and n-hentriacontoic; unsaturated acids such as the mono-ethenoid, caproleic, 10 decylenic, lauroleic, palmitoleic, oleic, elaidic, erucic, selacholeic and lumegueic acids; the polyethenoid acids such as linolelaidic, eleostearic, punicic, linolenic and moroetic acids; substituted acids such as ricinoleic, lanoceric and licanic acids; branched chain acids such as 2-methyldodecanoic, 14-ethyl hexadecanoic, 18-n-propyl heneicosanoic, 2 methyl tetracosanoic, 9-octyl heptadecanoic, 3,3-dimethyloctadecanoic and 2,9 dimethyloctadecanoic acids. Preferably R is a linear, aliphatic radical containing 10-17 carbon atoms. Most preferably, R is the hydrocarbon residue derived from stearic acid and has the formula (C H The following specific N-substituted fatty acid amides are illustrative of the different types which can be utilized in the compositions of this invention.

N-butyl,N- 2-carboxyethyl -6-octyl-9-dodecenamide N-methyl,N- (4-carboxybutyl -octadecanamide N- 3-carboxypropyl -2,7-dimethyl-3 1 O-octacosadienamide N-ethyl,N-(4-carboxybutyl) -12-n-hexyl octadecanamide N-methyl,N- Z-carboxyethyl -dodecanamide N- 5-carboxypentyl -3 ,9-diethyl-tetradecanamide N-ethyl-N-(S-carboxypentyl)-2,6,8-tripropyl undecanamide N-methyl,N- 2-carboxyethyl -octadecanamide N-ethyl,N- 3-carboxypropyl -heptadecanamide N-butyl,N- 3-carboxypropyl -undecanamicle N -pr0pyl,N- 3-carboxypropyl -octadecanamide N-propyl,N- (Z-carboxyethyl)-hexadecanamide N-butyl,N- (4-carboxybutyl -pentadecanamide N-butyl,N- (3-carboxypropyl -4,7,7-trimethyl-undecanamide N-butyl,N- (4-carboxybutyl -hexadosanamide N- (3-carboxypropyl) -triacontanamide N-(2-carboxyethyl)-10-decenamide N-methyl,N- (Z-carboxyethyl -9-octadecenamide N-propyl,N- (5-carboxypentyl) -2 l-triacontenamide N-ethyl,N-(Z-carboxyethyl)-12,14-dimethyl-9-hexadecenamide N- 3-carboxypropyl -15-pentyl-9-eicosenamide N-methyl,N-(Z-carboxyethyl) -9,12-octadecadienamide N-ethyl,N- 3-carboxypropyl) -9,1 1,13-octadecatrienamide N-methyl,N- 2-carboxyethyl) -9-dodecenamide N-methyl,N- (2-carboxyethyl -6-octadecenamide N-propyl,N-(5-carboxypentyl)-4,8,12,15,18,21-tetracosahexanenamide N-butyl,N-(3-carboxypropyl) -12-hexyl-6, IO-hexadecadienamide N-propyLN-(4-carboxybutyl)-6,14-dibutyl-9-octadecenamide N-ethyl,N- Z-carboxyethyl) -9-octadecynamide N-methyl,N- (2-carboxyethyl)-12-hydroxy-9-octadecenamide N-(2-carboxyethyl)-4-oxo-9,11,13-octadecatrienamide N-methyl,N-(2-carboxyethyl)-16-hydroxy-hexadecan amide and the sodium, potassium or lithium salts thereof.

The preparation of these amides is not critical to the practice of this invention. For example, these compounds can be prepared by replacing the hydroxyl group of an aliphatic fatty acid with an amine reactive ion such as chlorine and then reacting the acid chloride with an ester of an amino acid followed by saponification of the product to the acid. The alkali metal salts can be produced by reacting the ester with a suitable alkali metal base. Specifically, the preferred amide, stearoyl sarcosine, can be prepared by reacting stearic acid chloride with n-methyl ethyl glycinate followed by saponification.

The nitrogen containing compounds which can be utilized in the practice of this invention have the following structural formula:

W is selected from the group consisting of hydrogen and a lower alkyl radical containing up to about six carbon atoms. Preferably it is hydrogen. R" is hydrogen or a methyl radical. Preferably it is hydrogen. Z is a radical selected from the group consisting of Preferably Z is (RCO-). R is an aliphatic radical containing 10-30 carbon atoms and can be saturated or unsaturated, linear or branched chain, and can be substituted with a pendant oxygen atom such as a keto or hydroxy group or an ester linkage. It can be derived from the hydrocarbon residues of monocarboxylic fatty acids. Examples of monocarboxylic acids whose hydrocarbon residues can be utilized were heretofore set forth in the discussion of the N-substituted fatty acid amides. Preferably, R is a linear aliphatic radical containing 10-17 carbon atoms. Most preferably, R is a mixture of the hydro carbon residues derived from tallow which contains approximately 25 percent by weight palmitic acid, 35 percent by weight stearic acid and 45 percent by weight oleic acid. The hydrocarbon residues of other naturally occurring fatty acid mixtures such as coconut oil and soy bean oil can be utilized. 1 is an integer from 1-6 and preferably is 3.

It has been found that the marginal strippability is attained when the molecular weight of each alkoxy chain defined by y and y exceeds 1320 or when the moleculer weight of the alkoxy chain defined by v exceeds 220. It is also critical that the compound contain at least one alkoxy radical bonded to the nitrogen atom. Therefore, with respect to these limitations the value of y can range from 1 to about 30 and the value of y can range from zero to about 30. The value of v ranges from zero to about 10. Preferably, the alkoxy chains y and y are substantially equal in length. Preferably, y and y range from 1-5 and v ranges from 1-3. Most preferably, y, y and v are each 1.

Specific alkoxylated compounds wherein Z is equal to (RCO) include but are not limited to:

N-ethoxy-dodecanamide N,N-di (polyethoxy -octadecanamide N,N-di (polyethoxy -9, l 2-octadecadienamide N,N-di(polyethoxy)9,12,15-octadecatrienamide N,N-di(poly-1,2-propoxy)-6, 12-dipentyl-9-tetra decenamide N,N-di(poly-1,3-propoxy)-18-isobutyl-tetracosanamide N,N-di (polyethoxy) -hexadecanamide N,N-di (polyisobutoxy) -2-isopropyl- 1 Z-tridecenamide N,N-di(poly-1,4-butoxy)-6,9-dihydroxy-tetradecanamide N (poly-2,3-butoxy) -7,9,dioxo-5-hydr0xy-pentadecanamide N,N-di (ethoxy) -octadecanamide N,N-di [poly(2,3-butoxyethoXy) l-eicosanamide N,N-d-i [poly( 1,3-propoxy-1,2-propoxy) ]-12-hexadecynamide N,N-di (polymethoxy) 2,4,S-trimethyl-tetradecanamide Specific alkoxylated compounds wherein Z is RI! )v include but are not limited to:

N-(6-aminohexyl) ,N,N',N'-tri(poly-1,2-propoxy)-4,8-

diethyloctanediamine N- S-aminopropyl) ,N,N'-di (poly-2,3-butoxy) -9-hexadecenediamine N- (4-aminobutyl) ,N',N-di(poly-1,4-butoxy) -hexadecane diamine N-(S-aminopropyl),N,N,'N'-tri(poly-1,3-propoxy)- 8,12-dihydroxyhexadecane diamine N- 3-aminopropyl) ,N,N',N-tri (polyethoxy) -4-oxol 1- tetradecene diamine N- (Z-aminoethyLN- (poly-1,2-propoxy) ,N'- (poly-2,3-

butoxy) ,N- (polyethoxy) -3,6,8-trirnethyltetradecane diamine N-(aminomethyl)-N,N'-di(polyethoxy)-12-tetradecene diamine N- S-arninopentyl) -N,N,N'-tri (polymethoxy -octadecane diamine N- 3-aminopropyl -N,N',N-tri (polyethoxy) -octadecane diamine N-(4-aminobutyl) N,N,N'-tri(poly-1,3-propoxy)- 9,12-octadecadine diamine N- (S-aminopentyl) -N,N,N'-tri(polyethoxy) -4,8,12,15-

octadecatetraenoic diamine N- (aminomethyl) -N,N,N-tri (polyisobutoxy) -6-methyloctadecene diamine N- (Z-aminomethyl) -N,N-di(poly-1,2-propoxy) octadecane diamine N-(6-aminohexyl)-N,N,N'-tri(poly-1,4-butoxy)-9- octadecyne diamine N- 4-aminobutyl) -N,N,N-tri (polyethoxy l 4-pentylheptadecane diamine N- 3-aminopropyl) -N,N,N-tri (polyethoxy -octacosane diamine N- 3-aminoprophyl -N,N,N-tri ethoxy) -hexadecane diamine N- (B-arninopropyl)N,N,N-tri(propoxy- 1,3 -octadecane diamine The preparation of the nitrogen containing compound is not critical to the practice of this invention. For example, compounds wherein Z is (RCO-) can be prepared by alkoxylating the amide of the corresponding fatty acid. Compounds wherein Z is RN(CH can be prepared by reacting an N-aliphatic alkylene diamine having the formula (RNH-(CH NH with an alkylene oxide.

The wax component of this invention can be any wax which can be deposited upon a surface as a molten or solvent cut coating and thereafter changed into a solid phase by cooling or by evaporation of the solvent. These waxes can be of mineral, vegetable, animal or synthetic origin. Mixtures of various waxes can also be utilized. Exemplary of waxes having a mineral origin are the petroleum and hydrocarbon Waxes such as paratiin, microcrystalline, slack, ozocerite and montan Waxes. Waxes having a vegetable origin are carnauba, candelilla, Japan waxes and the like. Waxes having an animal origin include bees, Chinese, insect and similar waxes. In the animal and vegetable Waxes the main constituents are high molecular weight esters and saturated hydrocarbons and lesser amounts of alcohols and acids. Exemplary of the synthetic waxes include those produced by the esterification of polyhydric alcohols or by the hydrogenation of vegetable oils or those made by the Fischer- T ropsch synthesis or substituted waxes such as oxidized or chlorinated polyethylene wax.

The use of petroleum waxes represents a preferred embodiment of this invention. These waxes include paraffin waxes which have a melting point from about F. to about 200 F. and the microcrystalline waxes having a melting point from about 140 F. to 210 F. These Waxes may be fully refined and thus contain ;very small amounts of hydrocarbon oils or they may be semi-refined (slack waxes) and have hydrocarbon oil contents of up to about 30 percent. As more fully discussed hereafter, oils of this type may be added to the compositions of this invention to enhance the strippability of the coating in amounts ranging up to 20 percent of the total composition. Therefore, in determining an upper oil loading, the amount which is present due to the addition of a semirefined wax should be included.

The most preferred compositions of this invention utilize 100 percent by weight microcrystalline wax having a melting point ranging from 140 F. to 210 F. or a combination of petroleum waxes comprising from 20 to 80 percent by weight of a paraffin Wax having a melting point ranging from about F. to about 180 F. and from 80 to 20 percent of microcrystalline wax having a melting range from about F. to about 210 F. This wax mixture provides strippable coating which can be utilized in high temperature applications. Increasing the concentration of microcrystalline wax will impart a higher maximum use temperature and improve the ultimate physical strength While decreasing dimensional stability. With respect to paraffin waxes as a class the use of a non-normal parafiin wax imparts higher physical strength than the normal base paraffin waxes.

The copolymers which can be utilized in the practice of this invention are solid thermoplastic polymers produced by polymerizing a major amount of ethylene with a minor amount of vinyl acetate. These copolymers should be solid at ambient temperatures (i.e. 70 F.) and have a molecular weight sufficient to impart film strength without requiring excessive copolymer concentrations. The molecular weight can be further defined through the term melt index as determined by ASTM D 1238-62. In general, the operable copolymers have melt indexes of less than 500. Preferably, the melt index is less than 25 and most preferably, less than 5. Copolymers having melt indices as low as .5 have been prepared in the laboratory and have been found to impart outstanding strength characteristics. The vinyl acetate concentration in the copolymers can range from to 35 percent by weight. The higher concentration defines the practical limits of copolymer compatibility with the wax. Copolymers having a vinyl acetate content of less than 15 percent are more compatible but excessive copolymer concentrations are necessary to impart the desired film properties. The optimum film properties are obtained with copolymers having a vinyl acetate concentration ranging from to weight percent and are therefore preferred in the compositions of this invention.

The ethylene-vinyl acetate copolymers can be utilized in the practice of this invention alone or in conjunction with a compound which is a plasticizer for the copolymer. Exemplary compounds which are recognized as plasticizers for ethylenevinyl acetate copolymers include but are not limited to monomeric plasticizers such as dioctyl adipate, dioctyl phthalate, butyl phthalyl glycollate and aceto tributyl citrate or higher molecular weight plasticizers such as hydrocarbon oils, polyterpenes, polybutenes, epoxidized soy bean oil, coumarone-indene resins, polystyrene and organic carboxylic acids. These plasticizers in general have molecular weights of less than 3,000, are compatible with wax at the blending and application temperatures and have boiling or degradation temperatures which are higher than the temperatures incurred during coating. The coumarone-indene resins represent a preferred class of plasticizers. They are prepared by the catalytic polymerization of coal-tar, light-oil fractions boiling between 150 C. and 200 C. This fraction is commonly called crude heavy solvent and contains primarily indene, styrene, cyclopentadiene and their methyl homologs and minor amounts of coumarone. These resins have a softening point of less than 100 C. as determined by the ring and ball method described in ASTM Test Number D-36-62T. Preferably, this softening point is less than 50 C.

The use of organic carboxylic acids as plasticizers for the ethylene-vinyl acetate copolymers also represents a preferred embodiment in this invention. This carboxylic acid must be wax compatible, have an acid number in excess of about 20 and a molecular weight ranging from 150 to 3,000. Preferably, the acid number is in excess of 30. Compounds with low acid numbers and high molecular weights, i.e., oxidized polyethylene are not desirable because they increase the viscosity of the molten composition without imparting the desired properties. Any aliphatic, acyclic or aromatic acid having one or more car boxyl groups can be utilized. For example, dimerized and trimerized fatty acids, rosin acids and naphthoic acids can be also utilized.

The ethylene-vinyl acetate copolymer should be utilized in amounts sutficient to impart physical strength to the coatings thus allowing them to be Stripped from the surface as essentially continuous films. This requires a proper balance between the adhesive and cohesive forces with the adhesive force being less than the cohesive force. As the concentration of copolymer is increased, the physical strength of film is also increased. However, accompanying this improvement, is an increase in melt viscosity and in processing and material costs. Therefore, from both economic and processing viewpoints, the copolymer concentration should be the optimum required to impart the necessary strippability. A portion of the ethylene-vinyl acetate copolymer can be replaced by the plasticizers heretofore described. This copolymer-plasticizer mixture is hereafter described in the specification and claims as the poly-composition. This composition consists essentially of from 40 to percent by weight of an ethylene-vinyl acetate copolymer and from 0 to 60 percent by weight plasticizer. Most preferably, the plasticizer concentration ranges from 5 to 30 percent. The amount of polymeric composition which can be utilized in the compositions of this invention can range in amounts from 10 parts to 300 parts by weight of wax. Therefore, the copolymer can range in concentrations of from 4 to 300 parts per 100 parts of wax, and the plasticizer concentration can range from 0 to 180 parts per 100 parts wax. When the maximum plasticizer concentration of 180 parts is utilized, the maximum copolymer concentration is 120 parts. The most preferred concentration of polymeric composition ranges from 20 to parts per 100 parts of wax.

As previously stated, a hydrocarbon oil can be added to the composition of this invention to aid in strippability, impart a plasticizing effect and lower the hot melt viscosity. This hydrocarbon oil has a viscosity at 210 F. of greater than 25 SSU and preferably from about 35 to about 500 SSU at 210 F. A preferred oil is a highly refined n-parafiin petroleum oil having a viscosity of from 43 to 45 SSU at 210 F. The oils can be incorporated into the compositions of this invention in amounts ranging up to about 20 parts per 100 parts wax, however, excessive oil loading will greatly reduce tensile strength. Preferably, the oil concentration ranges up to about 15 parts and most preferably from 1 to 10 parts. As previously stated, some petroleum waxes commonly known as semi-refined waxes contain substantial amounts of oil. When these semi-refined waxes are utilized in this invention, its oil content should be taken into account in determining the maximum or optimum oil loading. In determining a common parts basis, the inherent oil content of semi-refined wax should be excluded.

Ingredients commonly added to wax or ethylene-vinyl acetate copolymers can be incorporated into the compositions of this invention in functional amounts without departing from the scope thereof. Examples of these ingredients include but are not limited to: heat and ultraviolet light stabilizers, inert fillers, secondary plasticizers, antiblocking agents, pigments and colorants, anti-oxidants, gloss stabilizers, viscosity-index improvers, solvents, antiscutf agents, etc.

The preparation of the compositions of this invention is not critical to the practice thereof and can be conducted under any suitable method. For example, these compositions can be prepared by heating the wax to a temperature above its melting point, adding the ethylene-vinyl acetate copolymer, stripping agent and other additives and agitating vigorously until a homogeneous hot melt is obtained.

When a plasticizer is utilized, it is preferable to incorporate the plasticizer into the melted wax prior to the addition of the copolymer in order to facilitate the dispersion of the copolymer. Similarly, a coating composition can be prepared by combining ingredients with a common solvent. A specific method for preparation is as follows: The waxes are melted together, any anti-oxidants or heat stabilizers are added and the melt is then brought to a temperature above about 275 F. The plasticizer, if it is not free flowing, is heated to about 275 F. and then added to the hot melt. The ethylene-vinyl acetate copolymer is then added to the melt accompanied by vigorous stirring while maintaining the melt temperature above about 275 F. After all of the copolymer has been added, the melt temperature is raised to about 300 F. and agitated until the copolymer and resins are completely dispersed. The desired release agents are then added.

Articles of manufacture can be prepared in any manner which results in a deposition of coating on its surface. For example, the articles may be dipped in a hot melt and cooled to allow the coating to solidify. This coating can also be deposited utilizing common coating processes such as curtain coating, roll coating and spray coating. The

16 same technique is followed when the solvent wax system cessive force. Slow removal rates were necessary and even is utilized. After coating, the solvent is evaporated. These then it came off 1n the form of small random p1eces. Poor coatings may be applied in any thickness. However, it is (P) denotes a coating which had high adhesion requiring necessary that the thickness provide sufficient strength in the application of excessive force at very slow removal the film to allow the film to remain intact during striprates. Small random pieces were obtained under these ping. Normally, coating thicknesses greater than 1 mil, conditions. Not strippable (l I.S.) means that the coating have this requisite strength. did not exhibit any strlpping charactenstics.

The following examples are given to illustrate the pre- TABLE I ferred embodiments of this invention and should not be Formulation NO 1 2 3 construed as limitations upon the invention. All parts are by Weight iii iiy iait eiisirataittssaivaa j 4193 45.93 4.193 EXAMPLE I :g01(1&1'OIgG-1nd?l}e resin 1g. :4 16. 4 y ocar on oi 6.6 01 1 N-lt'ttdftt The waxes of Table I were melted together and raised S 0 1.6 o to a temperature of 300 F. The coumar'one-indene resin f t F a 7 6 was heated to 275 F. and then added to the hot melt. The Anisfi iieatiii t?) 1170 F111; ii) 0 O U ethylene-vinyl eeeeee eeeelymee e e a t tartan???eieiei fiiiif; NS G NS melt w1th constant and vigorous ag1tat1on while maintaining a melt temperature above 0 F The melt temper The wax was a blend of 70.5 parts microcyrstalline wax having a o melting point of 175 F. (ASTM D-127) and 29.5 parts of a fully refined ature was raised to 300 F. after all of the copolymer paraffin wax having a melting point ranging from 150 to 155 F. (ASTM D-87). Both waxes had an oil content of less than 1 percent. had added F at that temperatule for 2 A11 ethylene-vinyl acetate copolymer having a bound vinyl-acetate approximately 90 minutes until all of the copolymer had content of 28 percent by weight and a melt index of 3.0 (ASTM D-1238- dissolved. The melt temperature was then lowered to 280 57,1)

3 Coumarone-indene resin having a ring and ball softening point of F. and the various release agents were added. The hot 38 0. (ASTM D36-627).

4 A solvent refined hydrocarbon oil comprised mainly of n-paraffins melt Was depos d Wlih a coating bar as 1 to 5 mll Coat having a viscosity index of 110 to 115 and a viscosity at 210 F. of 4346 ings on the surfaces of melamine-formaldehyde plaques. SSU.

a The coating was allowed to cool to 1.00m temperature and With reference to the geneial formula set forth in the specification, the

oleo sarcosine is defined as follows: R is the fatty residue oleic acid, R is j was l t d methyl n is 1 M is hydrogen. It was prepared by reactin oleic acid 24 hour i its sh lppab my chlor1dew1th ii-mcthyl amino acetic acid, ester and then sapdnifying the With other plaques, immediately after the coating was producttothe acid,

cooled, it was reheated to 170 F. for 10 minutes and al- 39 a lowed to cool. After 24 hours at ambient temperatures,

Table I demonstrates that the addition of an N-subsinppablhty evaluated The results we reported In 4 stituted fatty acid amide to the prior art compositions d1fferent categones:

greatly enhances the strippability. By comparing Formula- Exceuent (E) 15 us ed to deslgnate coatmg Wh1ch tion 3 with 2, it is demonstrated that even higher amounts could be easlly and rapldly remqved as f Smgle commuqus of the prior art stripping agents (oil) will not impart this film. Good (G) denotes a coating wh1ch could be eas1ly outstanding strippabflity. removed without the application of excessive force. However, at faster stripping rates it had a propensity to tear in P E II random fashion along the direction of the force and thus Th Compositions f T bl 11 were prepared d was removed as several large pieces. Fair (F) designates evaluated in accordance with the methods set forth in a coating which could be stripped only by applying ex- Example I.

TABLE II Formulation N0 4 6 6 7 8 9 10 11 Wax 100 100 100 100 100 100 100. Ethylene-vinyl acetate copolymer 42... 42.-. Coumarone indene resin 3 16.1 16.1. Hydrocarbon oil 4 3.2- 3.2 Release agent:

'lype Oleoyl sar- Oleoyl sar- Oleoyl sar- Oleoyl lin- Tallow di- Hydrogen- Aliphatic cosme cosine cosine oleoyl saramines ated talamine cosine amide Amount 0.... .8 1.6 1.6 1.6 1.6 1.6 1.6. Strippability properties:

24 hours after cooling to 70 F F-.. G to E G to E E E E E P, After heating coating to F. for 10 min- P-.- G E E E P utes and then cooling to 70 F. for 24 hours.

1 The wax was a blend of 67.7 parts of microcrystalline wax having a 9 The hydrogenated tallow amide had the following structural formula melting point of F. (ASIM D-127) and 32.3 parts of a microcrystallnegvax having a iirlieltigg piiintiirlange of liiO t? 19t5f11i (ztihsTlvll D427); 0t waxes were u yre he an a an oi eon en 0 ess an percen I a i and i As defined in Table I. E )CHQCHZOMH With reference to the general formula for the fatty acid amides set forth in the specification, stearoyl sarcosine is defined as follows: R is the fatty residue of stearic acid, R is methyl, n is 1, M is hydrogen. It (cHzoHzo) was prepared by reacting oleic acid chloride with n-methyl amino acetic y acid, ester and then saponifying the product to the acid.

7 A blend containing 55% oleic sarcosine and 45% linoleoyl sarcosine. wherein R is the hydrogenated fatty residue of tallow, 11 y equals 5 The oleic sarcosine was prepared as described in of Table I and the and the average molecular Weight was 498. Iinoleoyl sarcosine was prepared by reacting lineolic acid chloride with An aliphatic amine of the formula: n-methyl amino acetic acid, ester and saponfiying the product to the acid. R-NH2 B The diamine had the following structural formula: where1n R is saturated aliphatic radical containing from 15 to 20 carbon OHZOHZ OH atoms with an average carbon chain of 18 atoms.

R--NC H2-C H2CHz-N\ HzCHgOH CHzCHzOH wherein R is the fatty residue derived from tallow.

1 1 Table II demonstrates the various types of release agents which may be utilized in the practice of this invention and demonstrates their improvement over the prior art. Specifically, Formulations 5-8 illustrate the im- 12 (D) from to 20 parts of hydrocarbon oil having a viscosity at 210 F. in excess of 25 SSU. 2. A composition according to claim 1 wherein the wax is a petroleum wax.

proved strippability of coatings containing various N- 5 3- A c mpositionaccording to claim 2 Wherein the fatty acid amides. Formulations 9 and 10 illustrate the Petroleum Wax amlxture comprlslng from 2 080We1ght improved strippability of coatings with a nitrogen con- PQ P l WaX and from 80-20 Welght Percent taining compound. Formulation 4 is a prior art composimlcfocr Y Y tion containing hydrocarbon oil as the sole release agent. A P Q acfiofdlng clalm 1 Whereln P Formulation 11 contains an amine which has not been 10 polymfiflc COIIIPOSIUOH 1S pl'esfillt 111 all amount Tanglng alkoxylated. Both of these compositions do not provide from -110 P ti f t strippable coatings 5. A composition according to claim 1 wherein the EXAMPLE HI ethylene vinyl acetate copolymer has a vinyl acetate content ranging from -30 weight percent and a melt index In order to demonstrate the effect of plasticizers, blends 15 of less than 25. containing: 6. A composition according to claim 1 wherein the plasticizer is present in an amount ranging from 5-30 100 parts wax ht tb ht f h 1 81.8 parts of ethylene-vinyl acetate copolymer Welg percen Xwelg O 6 Po ymqnc Comp 7. A composition accordmg to claim 1 wherein the 45.5 parts plasticizer 2o plasticizer 1s a coumarone-indene resin having a softenmg were prepared 1n accordance with the method set forth in point of l than 50 C, Example I. The wax component contained 25 percent by 8, A composition accflfding to laim 1 wherei the weight microcrystalline wax having a melting point of plasticizer i n organic carboxylic a id, 175 F. (ASTM D-127) and 75 percent by weight of a 9. A composition according to claim 1 wherein the paraffin wax having a melting pomt of 135 F. (ASTM 25 hydrocarbon oil of Part D is present in an amount ranging D-87). The ethylene-vinyl acetate copolymer-28 percent from 4-10 parts and has a viscosity at 210 F. ranging by weight bound vinyl acetate has a melt index of 3.0 from -500 SSU. (ASTM D -l23857T) 10. A composition according to claim 1 wherein the The various plasticizers and their evaluations are set stripping agents defined in Part C are present in an amount forth in Table III. 30 ranging from 1-5 parts.

TABLE In Formulation No.

Commrone Epoxi- Poly indene Dlpctyl Dioctyl dized soy Poly- Plasticizer terpene resin adlpate Dhthalate bean oil butane Hot melt: vis. at 300 F. (cp.) 6,425 6,300 3,350 4, 280 s, 750 4, 250 Elongation, percent 105 166 16 36 33 Energy absorption factor, tt.-lbs./in 3 25.4 52.2 4.4 12.6 15,1 10

I claim: u 11. An article of manufacture comprising a solid object 1. A composition comprismg in parts by weight: having at least a portion of its surface coated with the (A) 100 parts of wax; composition of claim 1. (B) from 10 to 300 parts of a polymeric composition 45 12. A composition according to claim 1 wherein Z in consisting essentially of Part C has the structural formula:

(i) from 40-100 weight percent of an ethylenevinyl acetate copolymer wherein the vinyl acetate content ranges from 15-35 weight percent A and, I HCHz-0-) (ii) from 0-60 weight percent of a compound fl-IOW which is a plasticizer for the ethylene-vinyl acetam p y wherein R is an aliphatic hydrocarbon radical containing an amoufll 11fiic1e11t l0 p strlppabllltyfif 10-30 carbon atoms and t is an integer from 1-6 and a nitrogen containing compound having the following R" i hydrogen or a methyl radicaL Structural formula! 13. A composition according to claim 12 wherein the stripping agent has the following structural formula: -)HCHz-0 l30- 01110111011 R RNCHzCHrGHn-N I rigor-non 01120112011 wherein W is a radical selected from the group consisting of hydrogen and an alkyl radical containing zvhereltnnR 1s the aliphatic hydrocarbon group derived 1-6 carbon atoms, R" is hydrogen or a methyl radmm a ical, Z is a radical having the structural formula: No References cited.

z)r- MORRIS LIEBMAN, Primary Examiner HCH*O P. R. MICHL, Assistant Examiner l R o-1o-W wherein R is an aliphatic radical containing 10-30 carbon atoms and t is an integer from l-6, and R" is hydrogen or a methyl radical.

U.S. Cl. X.R. ll76 

